Does the risk of second primary cancer vary by race and ethnicity in survivors of early-onset colorectal cancer?
29,115 adults aged 18-49 years with stage 0-III early-onset colorectal cancer (EOCRC) diagnosed between 1992-2021 from the SEER 12 registry.
General population (for standardized incidence ratios)
Cumulative incidence of any second primary cancer (SPC) and second colorectal cancer (CRC)hard clinical
Survivors of early-onset colorectal cancer face a significantly increased risk of developing a second colorectal cancer, with notable racial and ethnic disparities, particularly affecting Hispanic White individuals.
Abstract Introduction: Early-onset colorectal cancer (EOCRC) incidence is rising sharply in the US, yet the long-term survivorship experience of this population remains poorly defined particularly among groups experiencing unequal cancer burden. Because racial and ethnic disparities persist in cancer-related exposures, treatment experiences, and survivorship care, the long-term probability of developing a second primary cancer (SPC) after EOCRC may also vary across population groups. We estimated risk of SPC by race and ethnicity to improve understanding of long-term survivorship following EOCRC. Methods: We used SEER 12 registry data to identify adults aged 18-49 years with stage 0-III EOCRC between 1992-2021. SPC was defined as any new primary cancer diagnosed ≥6 months after EOCRC. Accounting for competing risk of death, we estimated cumulative incidence of 1) any SPC and 2) second CRC by calendar time and attained age. Standardized incidence ratios (SIRs) compared risk to the general population. Analyses were stratified by sex and racial/ethnic groups. Results: Among 29,115 EOCRC survivors, 53.5% were male, and the racial/ethnic distribution was non-Hispanic White (NHW: 54%), non-Hispanic Black (NHB: 10.9%), Hispanic White (HW: 16.7%), Asian/Pacific Islander (API: 15%), and other (3.4%). Overall, 8.4% developed any SPC and 2.8% developed a second CRC. Cumulative incidence of any SPC did not differ significantly by race/ethnicity for men and women. Among men, SIRs for any SPC were 1.4 (95% CI: 1.3-1.5) for NHW, 1.4 (1.2-1.6) for NHB, 1.8 (1.5-2.1) for HW, and 2.4 (2.0-2.8) for API. Among women, SIRs were 1.3 (1.2-1.4) for NHW, 1.6 (1.3-1.9) for NHB, 1.6 (1.4-1.9) for HW, and 1.8 (1.6-2.1) for API. Cumulative incidence of second CRC differed significantly by race/ethnicity for men and women. At 25 years after diagnosis, cumulative incidence of second CRC was 2.8% (95% CI: 2.3-3.5) for NHW women; 4.6% (3.9-5.4) for NHW men; 5.5% (4.0-7.4) for NHB women; 4.0% (2.8-5.5) for NHB men; 5.9% (4.2-8.0) for HW women; 7.0% (5.3-9.1) for HW men; 4.0% (2.9-5.5) for API women; and 6.6% (4.8-8.9) for API men. By age 70, estimates were 2.9% (2.3-3.6) for NHW women, 4.7% (4.0-5.5) for NHW men, 5.6% (3.9-7.8) for NHB women, 4.6% (3.1-6.4) for NHB men, 4.9% (3.6-6.5) HW women, 6.7% (5.1-8.6) for HW men, 4.5% (3.1-6.3) for API women, and 6.1% (4.5-8.1) for API men. Second CRC SIRs showed similar patterns, with highest risks in HW men (SIR: 8.0; 95% CI: 6.3-10.0) and HW women (SIR: 7.1; 95% CI: 5.2-9.5). Conclusion: Despite no statistical differences in risk of any SPC, second CRC risk differed significantly by racial and ethnicity. HW men and women showed higher cumulative incidence over time, partly reflecting younger age at diagnosis and longer time at risk. Additional genetic, lifestyle, and care-related factors may contribute and warrant study to guide prevention and early detection in EOCRC survivors. Citation Format: Aniruddha B. Rathod, Caitlin C. Murphy, Sandi L. Pruitt. Risk of second cancer in survivors of early-onset colorectal cancer: racial and ethnic differences in a population-based study abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 900.
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Aniruddha Rathod
Caitlin C. Murphy
Sandi L. Pruitt
Cancer Research
University of Chicago
The University of Texas Southwestern Medical Center
University of Arkansas for Medical Sciences
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Rathod et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d1fdf7a79560c99a0a4542 — DOI: https://doi.org/10.1158/1538-7445.am2026-900